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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 1 (1968), S. 431-436 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 1 (1968), S. 463-464 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 14 (1981), S. 851-855 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
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  • 4
    Electronic Resource
    Electronic Resource
    Woodbury, NY : American Institute of Physics (AIP)
    Applied Physics Letters 65 (1994), S. 265-267 
    ISSN: 1077-3118
    Source: AIP Digital Archive
    Topics: Physics
    Notes: We report on poling of a low dielectric constant preimidized fluorinated fully aromatic guest-host polyimide nonlinear optical material including thermal stability of optical nonlinearities and waveguiding properties. We measured a second-harmonic coefficient (d33=4.9±0.5 pm/V at 1217 nm fundamental wavelength) which is accurately predicted by a thermodynamic model of poled polymers. The optical nonlinearity of a poled sample was thermally stable at 80 °C for over 300 h. Films were observed to have negative birefringence. Optical losses for slab waveguides in lowest order TE and TM modes were ≥7.7 dB/cm for doped waveguides at 800 nm wavelength and increased after poling.
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Journal of thermal analysis and calorimetry 46 (1996), S. 719-731 
    ISSN: 1572-8943
    Keywords: aromatic polyimide fiber ; as-spun fiber ; crystallization ; crystal structure ; crystal unit cell ; draw ratio ; dry-jet wet spinning ; isotropic solution ; modulus ; self-elongation ; tensile strength ; thermal shrinkage stress ; thermal shrinkage strain ; thermomechnical analysis ; triclinic ; wide angle X-ray diffraction ; zone drawing
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Three aromatic polyimides based on 3,3′,4,4′-biphenyl-tetracarboxylic dianhydride (BPDA) and three different diamines 2,2′-bis(trifluoromethyl)-4,4′-diaminobiphenyl (PFMB), 2,2′-dimethyl-4, 4′-diaminophenyl (DMB) or 3,3′-dimethylbenzidine (OTOL) have been synthesized. These polyimides are soluble in hotp-chlorophenol,m-cresol or other phenolic solvents. Fibers have been spun from isotropic solutions using a dry-jet wet spinning method. The as-spun fibers generally exhibit low tensile properties, and can be drawn at elevated temperatures (〉380° C) up to a draw ratio of 10 times. Remarkable increases in tensile strength and modulus are achieved after drawing and annealing. The crystal structures of highly drawn fibers were determinedvia wide angle X-ray diffraction (WAXD). The crystal unit cell lattices have been determined to be monoclinic for BPDA-PFMB and triclinic for both BPDA-DMB and BPDA-OTOL. Thermomechanical analysis (TMA) was used to measure thermal shrinkage stress and strain. A selfelongation has been found in the temperature region around 450°C. This phenomenon can be explained as resulting from the structural development in the fibers as evidencedvia WAXD observations.
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Journal of thermal analysis and calorimetry 46 (1996), S. 921-933 
    ISSN: 1572-8943
    Keywords: aromatic polyimide ; films ; in-plane orientation ; relaxation process ; thermal stability
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A new high molecular weight polyimide based on 4,4′-oxidiphthalic anhydride (ODPA) dianhydride and 2,2′-dimethyl-4,4′-diaminobiphenyl (DMB) diamine has been synthesizedvia a one-step polymerization method. This polyimide is soluble in phenolic solvents. Films from 7 to 30 μm thick were cast from the polymer solution and show in-plane orientation on a molecular scale detected by Fourier transform infrared spectroscopy experiments. This anisotropic structure leads to anisotropic optical properties arising from two different refractive indices along the inplane and out-of-plane directions. ODPA DMB possesses high thermal and thermo-oxidative stability. The glass transition temperature has been determined to be 298 °C. Dynamic mechanical analyses show two relaxation processes appearing above room temperature: the β- and the α-relaxation processes. The α-relaxation corresponds to the glass transition while the β-relaxation is a secondary relaxation process associated with the non-cooperative subsegmental motion.
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Journal of thermal analysis and calorimetry 47 (1996), S. 957-973 
    ISSN: 1572-8943
    Keywords: DSC ; Gibbs energy ; liquid crystalline polyethers
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A series of polyethers have been synthesized from 1-(4-hydroxy-4′-biphenyl)-2-(4-hydroxyphenyl)propane and α, Ω-dibromoalkanes having different numbers of methylene units [TPPs]. Both odd- and even-numbered TPPs [TPP(n=odd)s and TPP(n=even)s) exhibit multiple transitions during cooling and heating and they show little supercooling dependence, indicating close-to-equilibrium nature of these transitions. Combining the structural characterization obtainedvia wide angle X-ray diffraction powder and fiber patterns at different temperatures and the morphological observations from microscopy techniques, not only the nematic liquid crystalline phase but also highly ordered smecticF, smectic crystalG andH phases have been identified. The phase diagrams for both TPP(n=odd)s and TPP(n=even)s have been constructed [1–3]. Thermodynamic properties (enthalpy and entropy changes) during these transitions are studied based on differential scanning calorimetry experiments. The contributions of the mesogenic groups and methylene units to each ordering process can be separated and they indicate the characteristics of these processes thereby providing estimations of the transition types.
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 31 (1996), S. 4423-4431 
    ISSN: 1573-4803
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract A new polyimide has been synthesized from 3,3′,4,4′-biphenyltetracarboxylic dianhydride (BPDA) and 2,2′-dimethyl-4,4′-diaminobiphenyl (DMB). A high-strength, high-modulus, high-temperature fibre has been developed from this polyimide via a dry-jet wet spinning method. The tensile strength of BPDA-DMB fibres is 3.3 GPa and the tensile modulus is around 130 GPa. The compressive strength of the fibres has been investigated through a tensile recoil test (TRT), while the fibre morphology after compression has been studied via polarized light microscopy (PLM) and scanning electron microscopy (SEM). From the TRT measurements, we have observed that the compressive strength of this fibre is 665 (±5) MPa, which is higher than those of other aromatic polymer fibres. The effect of fibre diameter on the compressive strength of BPDA-DMB fibres is not substantial. The critical compressive strain for this fibre at which the kink bands start appearing under the observation of PLM is at 0.51–0.54%. Subglass relaxation processes have been observed and the measure of an apparent relaxation strength may serve as one of the factors which significantly affect the compressive strength of the fibres. Tensile tests of pre-compressed fibres reveal a continuous loss in tensile strength (up to 30%) with increasing the compressive strain (up to 2.6%). PLM and SEM observations show that during the compression BPDA-DMB fibres form regularly-spaced kink bands at ±60 ° (±2 °) with respect to the fibre axis. The kink band density initially increases with the compressive strain, and reaches a maximum at around 1.1%. Further increase of the compressive strain decreases this density due to the merge of the neighbouring bands. The size of kink bands also correspondingly increases within this compressive strain region. The morphological observation via SEM implies the existence of a skin-core structure and microfibrillar texture which are common features in polymer fibres.
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  • 9
    ISSN: 1572-8943
    Keywords: heterocyclic polymers ; mechanical properties ; thermal degradation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The thermal mechanical properties and degradation behaviors were studied on fibers prepared from two high-performance, heterocyclic polymers, poly(p-phenylenebenzobisthiazole) (PBZT) and poly(p-phenylenebenzobisoxazole) (PBZO). Our research demonstrated that these two fibers exhibited excellent mechanical properties and outstanding thermal and thermo-oxidative stability. Their long-term mechanical tensile performance at high temperatures was found to be critically associated with the stability of the C—O or C—S linkage at the heterocyclic rings on these polymers' backbones. PBZO fibers with the C—O linkages displayed substantially higher thermal stability compared to PBZT containing C—S linkages. High resolution pyrolysis-gas chromatography/mass spectrometry provided the information of the pyrolyzates' compositions and distributions as well as their relationships with the structures of PBZT and PBZO. Based on the analysis of the compositions and distributions of all pyrolyzates at different temperatures, it was found that the thermal degradation mechanisms for both of these heterocyclic polymers were identical. Kevlar®-49 fibers were also studied under the same experimental conditions in order to make a comparison of thermo-oxidative stability and long-term mechanical performance at high temperatures with PBZO and PBZT fibers. The data of two high-performance aromatic polyimide fibers were also included as references.
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  • 10
    ISSN: 1573-4803
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Physical origins of banded structures appearing on different length scales have been investigated using polarized light and atomic force microscopies (PLM and AFM), polarized Fourier Transform infrared spectroscopy (FT-IR) and wide angle X-ray diffraction (WAXD) in a combined main-chain/side-chain liquid crystalline (LC) polyester, PEFBP(n). This series of PEFBP(n) polymers was synthesized from the polycondensation of 2,2′-bis(trifluoromethyl)-4,4′-biphenyldicarbonyl chloride with 2,2′-bis{ω-[4-(4-cyanophenyl)-phenyoxy]-n-alkoxycarbonyl]}-4,4′-biphenyl diol. In this paper, we focus on one polymer [PEFBP(n = 11)] of this series to illustrate the band structural formation on different length scales during the evolution from liquid crystal to crystalline states. Alternating bands of the films mechanically-sheared at 190 °C are formed with a spacing of 3 ± 0.5 μm in PLM, and recognized to be primary bands. PLM and AFM results show that these bands are seen due to the change of optical birefringence constructed mainly by alternating film thickness (and thus, retardation). Based on polarized FT-IR results, both the backbones and side chains of the polymers are orientated parallel to the shear direction. Secondary fibrillar bands develop within the primary bands after the sample is subsequently crystallized at 105 °C. These bands show a zigzag arrangement and possess a lateral size of 250 ± 50 nm determined by AFM. High resolution AFM observations illustrate that these bands consist of aggregated edge-on crystal lamellae having a thickness of approximately 20 nm. The lamellar crystals are assembled together and lie across the film thickness direction. The mechanism for the formation of these secondary zigzag bands originates from the expansion of the lattice dimension along the chain direction on a molecular scale during the nematic to crystalline phase transition and crystallization in the partially confined LC primary bands, which form macroscopic zigzag buckling.
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